KR100351571B1 - Method of controlling dust - Google Patents
Method of controlling dust Download PDFInfo
- Publication number
- KR100351571B1 KR100351571B1 KR1019960701232A KR19960701232A KR100351571B1 KR 100351571 B1 KR100351571 B1 KR 100351571B1 KR 1019960701232 A KR1019960701232 A KR 1019960701232A KR 19960701232 A KR19960701232 A KR 19960701232A KR 100351571 B1 KR100351571 B1 KR 100351571B1
- Authority
- KR
- South Korea
- Prior art keywords
- dust
- ptfe
- emulsion
- polytetrafluoroethylene
- powdered material
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B40/00—Processes, in general, for influencing or modifying the properties of mortars, concrete or artificial stone compositions, e.g. their setting or hardening ability
- C04B40/0028—Aspects relating to the mixing step of the mortar preparation
- C04B40/0039—Premixtures of ingredients
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
- C04B28/02—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing hydraulic cements other than calcium sulfates
-
- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05G—MIXTURES OF FERTILISERS COVERED INDIVIDUALLY BY DIFFERENT SUBCLASSES OF CLASS C05; MIXTURES OF ONE OR MORE FERTILISERS WITH MATERIALS NOT HAVING A SPECIFIC FERTILISING ACTIVITY, e.g. PESTICIDES, SOIL-CONDITIONERS, WETTING AGENTS; FERTILISERS CHARACTERISED BY THEIR FORM
- C05G3/00—Mixtures of one or more fertilisers with additives not having a specially fertilising activity
- C05G3/20—Mixtures of one or more fertilisers with additives not having a specially fertilising activity for preventing the fertilisers being reduced to powder; Anti-dusting additives
-
- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05G—MIXTURES OF FERTILISERS COVERED INDIVIDUALLY BY DIFFERENT SUBCLASSES OF CLASS C05; MIXTURES OF ONE OR MORE FERTILISERS WITH MATERIALS NOT HAVING A SPECIFIC FERTILISING ACTIVITY, e.g. PESTICIDES, SOIL-CONDITIONERS, WETTING AGENTS; FERTILISERS CHARACTERISED BY THEIR FORM
- C05G3/00—Mixtures of one or more fertilisers with additives not having a specially fertilising activity
- C05G3/80—Soil conditioners
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/22—Materials not provided for elsewhere for dust-laying or dust-absorbing
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2103/00—Function or property of ingredients for mortars, concrete or artificial stone
- C04B2103/0068—Ingredients with a function or property not provided for elsewhere in C04B2103/00
- C04B2103/0075—Anti-dusting agents
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Materials Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Structural Engineering (AREA)
- Pest Control & Pesticides (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Soil Sciences (AREA)
- Colloid Chemistry (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
Abstract
분말상물질을 폴리테트라플루오로에틸렌과 혼합하고, 혼합물을 약 20 내지 200℃의 온도에서 압축- 전단 작용을 시키고, 그것에 의해 상기 폴리테트라플루오로에틸렌을 피브릴화하여 분말상물질의 분진을 억제함에 의한 분말상물질의 분진억제방법에 있어서, 본 방법은 유화안정제로서 탄화수소계 음이온 계면활성제를 폴리테트라플루오로에틸렌에 대하여 1.0wt%이상 함유하고, 2.20이하의 비중과 0.10-0.50μ의 평균입경을 가지는 테트라플루오로에틸렌의 단독 중합체의 수성유제를 사용하는 것을 특징으로 하는 분말상물질의 분진억제방법.By mixing the powdered material with polytetrafluoroethylene and subjecting the mixture to a compressive-shearing action at a temperature of about 20 to 200 ° C, thereby fibrillating the polytetrafluoroethylene to suppress dust of the powdered material. In the dust suppression method for powdered materials, the present method is an emulsifying stabilizer containing a hydrocarbon-based anionic surfactant of 1.0 wt% or more with respect to polytetrafluoroethylene, and having a specific gravity of 2.20 or less and an average particle diameter of 0.10-0.50 μ . A method for controlling dust of a powdery substance, characterized by using an aqueous emulsion of a homopolymer of fluoroethylene.
Description
발명의 상세한 설명Detailed description of the invention
일본국 특허공보 제52-32877호는 분말상물질을 PTFE와 혼합하고, 혼합물을 20 내지 200℃의 온도에서 압축- 전단하고, 그것에 의해 PTFE를 피브릴화하여 분말상물질의 분진을 억제함으로써 분말상물질의 분진을 억제하기 위한 방법을 개시한다.Japanese Patent Application Laid-Open No. 52-32877 discloses a powdered material by mixing powdered material with PTFE, compressing and shearing the mixture at a temperature of 20 to 200 ° C, thereby fibrillating PTFE to suppress dust of the powdered material. Disclosed is a method for suppressing dust.
거기에 개시된 PTFE는 TEFLON?6 또는 TEFLON?30으로 표시되는 테트라플루오로에틸렌의 미세분말 또는 유제형태의 단독 중합체와 또한 TEFLON?6C 또는 TEFLON?64로 표시되는 테트라플루오로에틸렌의 미세분말 또는 유제형태의 변성 중합체를 포함한다.The PTFE disclosed therein is TEFLON ? 6 or TEFLON ? Homopolymer in the form of fine powder or emulsion of tetrafluoroethylene represented by 30 and also TEFLON ? 6C or TEFLON ? It includes a modified polymer in the form of fine powder or emulsion of tetrafluoroethylene represented by 64.
그후에 "TEFLON?K-10" (PTFE 미세분말) 및 "TEFLON?K-20" (PTFE 유제) 이 개발되어, 방진용도를 위해 출시되고 있다.After that "TEFLON? K-10" ( PTFE fine powder) and "TEFLON? K-20" ( PTFE emulsion) has been developed, which are being released for vibration applications.
그리고 상기 PTFE에 있어서, 불충분한 피브릴화, 원섬유의 불만족한 강도 및 분말상물질중의 PTFE의 비균일한 분포로 인하여 방진효과의 변동이 발생한다.In the PTFE, fluctuations in the dustproof effect occur due to insufficient fibrillation, unsatisfactory strength of raw fibers, and non-uniform distribution of PTFE in powdery materials.
특히 유제타입의 방진제의 경우, 그것의 이송, 계량, 희석 동안의 기계적 작용에 의해 초래되는 PTFE 콜로이드 입자의 석출 및 응집과 같은 유제 자체에 관련된 문제점이 있으며, 이것은 파이프, 펌프, 오리피스 등의 막힘을 초래하고, 또한 유제중의 PTFE의 농도 감소를 초래하여 분말상물질에 대한 PTFE의 틀린 혼합비율을 초래한다.Particularly in the case of emulsion type dustproof agents, there is a problem related to the emulsion itself, such as precipitation and aggregation of PTFE colloidal particles caused by mechanical action during its transport, metering, and dilution, which causes clogging of pipes, pumps, orifices, etc. And a decrease in the concentration of PTFE in the emulsion, resulting in an incorrect mixing ratio of PTFE to powdery material.
더욱이 비료, 토질 안정제 및 석탄재등의 매립재료와 같은 분말상물질을 위해 다량의 유제타입 방진제를 사용한 결과로서, 유화안정제로서 사용된 계면활성제는 지하수, 호수, 하천등의 오염물이 될 가능성이 있다.Moreover, as a result of using a large amount of emulsion type dustproof agents for powdery materials such as fertilizers, soil stabilizers, and landfill materials such as coal ash, the surfactants used as emulsifying stabilizers may be contaminants such as groundwater, lakes and rivers.
본 발명의 목적은 테트라플루오로에틸렌 단독 중합체의 수성유제를 사용하여 분말상물질의 분진을 효과적으로 억제하기 위한 방법을 제공하는 것이며, 이 유제는 매우 안정하고 지하수의 오염물이될 가능성이 적다.It is an object of the present invention to provide a method for effectively suppressing dust of powdery materials using an aqueous emulsion of tetrafluoroethylene homopolymer, which is very stable and unlikely to be a contaminant of groundwater.
발명의 개시Disclosure of the Invention
분말상물질을 PTFE와 혼합하고, 혼합물을 20 내지 200℃의 온도에서 압축- 전단 작용을 시키고, 그것에 의해 PTFE를 피브릴화하여 분말상물질의 분진을 억제함으로써 분말상물질의 분진을 억제하기 위한 방법의 본 발명에 따르면, 본 방법은 유화안정제로서 탄화수소계 음이온 계면활성제를 PTFE에 대하여 1.0wt%이상 함유하고, 2.20이하의 비중과 0.10-0.50μ의 평균입경을 가지는 테트라플루오로에틸렌의 단독 중합체의 수성유제를 사용하는 것을 특징으로 한다.Example of a method for suppressing dust of a powdery substance by mixing the powdery substance with PTFE, compressing and shearing the mixture at a temperature of 20 to 200 ° C, thereby fibrillating PTFE to suppress dust of the powdery substance According to the invention, the present method is an aqueous emulsion of a homopolymer of tetrafluoroethylene containing 1.0 wt% or more of a hydrocarbon-based anionic surfactant as PTFE, and having a specific gravity of 2.20 or less and an average particle diameter of 0.10-0.50 μ . It characterized in that to use.
발명을 실시하기 위한 최상의 방식Best way to carry out the invention
비록 PTFE는 테트라플루오로에틸렌의 소위 단독 중합체와 테트라플루오로에틸렌 및 1% 이하의 공단량체의 공중합체인 소위 변성 중합체를 포함하지만, 본 발명에 유용한 PTFE는 단독 중합체이다. 변형된 PTFE 중합체의 수성유제를 사용한 방진제는 본 발명의 방진효과 보다 낮은 방진효과를 나타내며, 동일한 효과를 보여주기 위해 자주 50% 이상의 과량의 방진제를 필요로 한다.Although PTFE includes a so-called modified polymer that is a copolymer of tetrafluoroethylene and a so-called homopolymer of tetrafluoroethylene and up to 1% comonomer, PTFE useful in the present invention is a homopolymer. The anti-vibration agent using the aqueous emulsion of the modified PTFE polymer shows a lower dust-proofing effect than the dust-proofing effect of the present invention, and often requires an excess of 50% dust-proofing agent to show the same effect.
본 발명에 적합한 PTFE는 0.10-0.50μ, 바람직하게는 0.10-0.30μ의 범위의 평균입경을 가지고, 2.20이하, 바람직하게는 2.18 이하의 비중을 가진다. 0.10μ미만의 평균입경을 갖는 콜로이드 입자는 열등한 방진효과를 가져오고, 0.50μ초과의 입자는 불안정유제를 초래한다. 2.20 초과의 비중을 갖는 PTFE는 열등한 방진효과를 가져온다.PTFE suitable for the present invention has an average particle diameter in the range of 0.10-0.50 µ , preferably 0.10-0.30 µ , and has a specific gravity of 2.20 or less, preferably 2.18 or less. Colloidal particles having an average particle diameter of less than 0.10 μ have an inferior dustproof effect, and particles larger than 0.50 μ cause an instability emulsion. PTFE with a specific gravity above 2.20 has an inferior dustproof effect.
PTFE 입자의 평균입경은 원심침강법에 의해 결정할 수 있으며, 본 발명을 위해서는 원심침강식 입도분포 측정장치(Shimazu Corp.; SA-CP4L)를 사용했다. 비중은 미국특허 제 3,142,665호에 기술된 방법에 따라 응집된 콜로이드 입자를 사용하여 측정했다.The average particle diameter of the PTFE particles can be determined by the centrifugal sedimentation method. For the present invention, a centrifugal sedimentation particle size distribution analyzer (Shimazu Corp .; SA-CP4L) was used. Specific gravity was measured using agglomerated colloidal particles according to the method described in US Pat. No. 3,142,665.
상기 PTFE 입자는 미국특허 제 2,559,752호에 기술된 바와 같은 유화중합법에 의해 얻을 수 있으며, 여기서 테트라플루오로에틸렌을 수용성 중합개시제 및 유화안정제로서 소수성 플루오로알킬 라디칼을 갖는 음이온 계면활성제를 함유하는 수성매체에 압력하에 채워서 중합되어 PTFE 수성유제를 형성하도록 한다. 그러나 그렇게 얻어진 PTFE 수성유제는 안정성에서 열등하기 때문에, 유제는 또한 유화안정제의 첨가를 필요로 한다.The PTFE particles can be obtained by emulsion polymerization as described in US Pat. No. 2,559,752, wherein tetrafluoroethylene is used as an aqueous surfactant containing an anionic surfactant having a hydrophobic fluoroalkyl radical as a water soluble polymerization initiator and an emulsion stabilizer. The medium is filled under pressure to polymerize to form PTFE aqueous emulsion. However, because the PTFE aqueous emulsions so obtained are inferior in stability, they also require the addition of emulsifiers.
본 발명에 사용되는 유화안정제는 탄화수소계 음이온 계면활성제이며, 이것은 토양의 본질적 성분인 칼슘, 알루미늄 및 철과 반응함으로써 물에 불용성 또는 난용성 염을 형성하기 때문에 계면활성제에 의해 유발되는 하천, 호수 및 지하수의 오염을 회피한다. 고급지방산의 염, 고급알코올황산에스테르의 염, 지방오일황산에스테르의 염, 지방족 알코올인산에스테르의 염, 이염기지방산에스테르술폰산의 염, 알킬아릴술폰산의 염 등과 같은 탄화수소계 음이온 계면활성제에 대한 언급이 있다. 그것들 중에 -(CH2CH2O)1-6-및 C8-11알킬을 갖는 폴리옥시애틸렌- 알킬페닐에테르- 에틸렌술폰산, C10-12알킬을 갖는 알킬벤젠술폰산과 C8-10알킬을 갖는 디알킬술포숙신산에스테르의 Na, K, Li 및 NH4염이 높은 기계적 안정성을 갖는 PTFE 수성유제를 제공하기에 바람직한 것으로서 예시되어 있다. 첨가될 유화안정제의 양은 PTFE의 1.0wt%이상, 바람직하게는 1.5-5wt%이다. 1.0wt% 미만의 양은 불만족스럽게 안정화된 수성 PTFE 유제를 제공하며, 10wt% 이상의 양은 비경제적이다.Emulsifying stabilizers used in the present invention are hydrocarbon-based anionic surfactants, which are caused by surfactants because they form insoluble or sparingly soluble salts in water by reacting with calcium, aluminum and iron, which are essential components of the soil. Avoid groundwater contamination. References are made to hydrocarbon-based anionic surfactants such as salts of higher fatty acids, salts of higher alcohol sulfate esters, salts of fatty oil sulfate esters, salts of aliphatic alcohol phosphate esters, salts of dibasic fatty acid ester sulfonic acids, salts of alkylarylsulfonic acids, and the like. have. Among them are poly (oxystyrene-alkylphenylether-ethylenesulfonic acid having- (CH 2 CH 2 O) 1-6- and C 8-11 alkyl, alkylbenzenesulfonic acid having C 10-12 alkyl and C 8-10 alkyl The Na, K, Li and NH 4 salts of the dialkylsulfosuccinic acid esters having exemplified are preferred as to provide a PTFE aqueous emulsion having high mechanical stability. The amount of emulsifier stabilizer to be added is at least 1.0 wt%, preferably 1.5-5 wt% of PTFE. An amount of less than 1.0 wt% provides an unsatisfactory stabilized aqueous PTFE emulsion, with an amount of more than 10 wt% being uneconomical.
비록 유제중 PTFE의 함량은 특별히 제한되지 않지만, 낮은 함량이 분진발생물질에로의 PTFE의 향상된 분산을 위해 바람직하다. 한편 높은 함량은 유제의 수송비용을 감소할 수 있다. 그래서 PTFE의 함량은 보통 10wt% 이상이고, 바람직하게는 20-70wt%이다. 더 높은 함량은 유제안정성을 저하시키므로 바람직하지 않다. 따라서 상업적 방진제는 20-70wt%의 PTFE 함량을 가지고, 그 제품을 분진발생물질과 혼합하기 전에 물로 희석하여 5wt% 이하의 PTFE 함량을 만드는 것이 일반적이다.Although the content of PTFE in the emulsion is not particularly limited, a low content is preferred for improved dispersion of PTFE into dust generating materials. On the other hand, a high content can reduce the transportation cost of the emulsion. So the content of PTFE is usually 10wt% or more, preferably 20-70wt%. Higher content is undesirable since it lowers emulsion stability. Thus, commercial dustproofers have a PTFE content of 20-70wt%, and the product is usually diluted with water to produce a PTFE content of less than 5wt% before mixing with the dust generating material.
수성 PTFE 유제의 기계적 안정성은 유제의 고속 교반 동안 충돌에 의해 초래되는 회합된 콜로이드 입자의 외견상 크기의 증가 비율을 관찰함으로써 평가할 수 있다. 그리고 교반에 의해 초래되는 응집된 콜로이드 입자의 일부분은 교반 로터 및 용기의 벽에 부착하거나, 유제로 부터 분리된 플록(flock) 을 형성한다. 이러한 현상의 발생하에, 유제는 유제에 남아 있는 콜로이드 입자의 크기의 변화에도 불구하고, 열등한 안정성을 갖는 것으로 간주된다.The mechanical stability of an aqueous PTFE emulsion can be assessed by observing the rate of increase in the apparent size of the associated colloidal particles caused by the collision during the high speed agitation of the emulsion. And a portion of the agglomerated colloidal particles caused by the agitation adheres to the stir rotor and the walls of the vessel or forms a flock separated from the emulsion. Under the occurrence of this phenomenon, the emulsion is considered to have inferior stability despite the change in the size of the colloidal particles remaining in the emulsion.
본 발명에서, 기계적 안정성은 다음 절차에 따라 측정된 입경 증가율에 의해 결정한다. 60mm 내경의 비이커내로 S1의 평균입경를 갖는 200㎖의 유제를 채운다.In the present invention, the mechanical stability is determined by the rate of particle size increase measured according to the following procedure. Into a 60 mm inner diameter beaker is filled 200 ml of an emulsion having an average particle diameter of S 1 .
발전기에 달린 축을 갖는 교반기(URTRA-TURRAX: JANKE 및 KUNKEL GMBH 및 Co. KG제) 를 설치하여 축이 비이커의 바닥 15mm 위에 있고, 5mm 편심되게 한다.An agitator (URTRA-TURRAX: manufactured by JANKE and KUNKEL GMBH and Co. KG) with a shaft attached to the generator is installed so that the shaft is 15 mm above the bottom of the beaker and 5 mm eccentric.
로터를 5분 동안 20,500rpm으로 회전시킨후, 유제의 평균입경(S2) 를 측정한다.After rotating the rotor at 20,500 rpm for 5 minutes, the average particle diameter (S 2 ) of the emulsion is measured.
입경 증가율은 다음에 따라 계산한다:The particle growth rate is calculated as follows:
입경 증가율(%) = (S2-S1)/ S1x100% Increase in particle size = (S 2 -S 1 ) / S 1 x100
기계적 안정성은 다음과 같이 평가한다:Mechanical stability is evaluated as follows:
"입경 증가율" 이 > 0% - < 5% 인때에는 양호,Good when "particle growth rate" is> 0%-<5%,
"입경 증가율" 이 ≥5% - < 10%인때에는 보통,Usually when the "particle growth rate" is ≥5%-<10%,
"입경 증가율" 이 ≥10% 인때에는 약함.Weak when the "particle growth rate" is ≥10%.
더욱이 교반에 의해 다량의 응집물이 나타났을때 약함이 평가된다.Furthermore, weakness is assessed when a large amount of aggregates are displayed by stirring.
분진억제율은 다음 절차에 따라 결정한다. 34cm높이 x 23cm 폭 x 1.8m 길이의 상자형 공기도관의 한쪽 끝으로 부터 송풍기를 사용하여 0.25m/초의 속도를 갖는 공기를 통과시킨다. 도관의 출구 위에 설치된 깔대기의 2cm 직경 출구를 통해, 방진된 소석회를 일정한 속도(3-10g/ 초) 로 낙하시키고, 출구밑에 놓인 34cmx34cm 접시상에 축적된 석회를 방진된 석회의 양으로 간주한다. 분진억제율은 다음과 같이 계산한다:Dust suppression rate is determined by the following procedure. From one end of a 34 cm high x 23 cm wide x 1.8 m long box air duct, use a blower to pass air at a rate of 0.25 m / sec. Through the 2 cm diameter outlet of the funnel installed above the outlet of the conduit, the dust-free lime is dropped at a constant rate (3-10 g / sec), and the lime accumulated on the 34 cm x 34 cm dish below the outlet is considered to be the amount of dust lime. The dust suppression rate is calculated as follows:
분진억제율(%) = 방진된 석회의 중량/ 낙하된 석회의 중량 x 100Dust Inhibition Rate (%) = Weight of Dust Lime / Weight of Falled Lime x 100
시험 1Test 1
표 1 및 표 2에 언급된 각각 18㎖의 수성 PTFE 유제 A, B, C, D, E, F, G 또는 H를 800㎖의 물과 혼합하고, 혼합물을 5mm 이하의 입경를 갖는 20kg의 생석회상에 각각 분무했다. PTFE 유제와 혼합된 생석회를 50리터 회반죽 혼합기에서 2분 동안 압축- 전단시켰으며, 이동안 생석회 및 수성유제중의 수분 사이의 반응 때문에 혼합기내 내용물의 온도가 올라 갔으며, 수증기를 발생시켜 수분을 상당히 제거했다.Mix 18 ml of aqueous PTFE emulsion A, B, C, D, E, F, G or H mentioned in Table 1 and Table 2 with 800 ml of water and mix the mixture 20 kg of quicklime with a particle diameter of 5 mm or less. Sprayed on each. The quicklime mixed with PTFE emulsion was pressed and sheared for 2 minutes in a 50 liter plaster mixer, during which the temperature in the mixer increased due to the reaction between the quicklime and the water in the aqueous emulsion, generating water vapor Removed quite a bit.
그래서 생석회 및 수분 사이의 반응에 의해 형성되는 소량의 소석회를 함유하는 방진된 생석회를 얻었다. 그렇게 얻어진 각각의 생석회 샘플에 대해 분진억제율을 측정했으며, 그 결과는 표 1 및 표 2에 보여진다. 본 발명 A, B, C 또는 D의 수성 PTFE 유제를 사용한 각각의 실시예는 2.20 초과의 PTFE 입자의 비중을 갖는 유제 F 또는 변형된 PTFE의 수성유제인 유제 G를 사용한 비교예의 분진억제율 보다 더 높은 분진억제율을 가리킨다는 것이 밝혀졌다. 더욱이 0.5wt%의 유화안정제를함유하는 유제 E를 사용한 비교예는 유제의 응집 때문에 분무 불가능 했다.Thus, a dustproof quicklime containing a small amount of slaked lime formed by the reaction between quicklime and moisture was obtained. The dust inhibition rate was measured for each of the quicklime samples thus obtained, and the results are shown in Tables 1 and 2. Each example using the aqueous PTFE emulsion of the present invention A, B, C or D has a higher dust than the dust suppression rate of the emulsion F having a specific gravity of more than 2.20 PTFE particles or the comparative example using emulsion G, an aqueous emulsion of modified PTFE. It was found to indicate inhibition rate. Moreover, the comparative example using the emulsion E containing 0.5 wt% of emulsion stabilizer was impossible to spray due to the aggregation of the emulsion.
시험 2Test 2
포틀랜드 시멘트는 시멘트 클링커를 적당한 양의 석고와 혼합하고, 혼합물을 마무리 제분기에서 분쇄함으로써 제조했다. 제품은 88μ표준망(sieve) 상에서 1.1% 잔류물의 입도, Blaine 방법에 의해 측정된 3300㎠/g의 비표면적과 100-120℃의 온도를 가졌다. 마무리 제분기로 부터의 100-120℃의 포틀랜드 시멘트를 용적식 연속공급기로 5T/H의 속도로 쌍축반전식 패들혼합기(15rpm) 에 채웠다.Portland cement was prepared by mixing cement clinker with an appropriate amount of gypsum and grinding the mixture in a finishing mill. The product had a particle size of 1.1% residue on a 88 μ sieve, a specific surface area of 3300 cm 2 / g and a temperature of 100-120 ° C. measured by the Blaine method. Portland cement at 100-120 ° C. from the finishing mill was charged to a twin-spindle paddle mixer (15 rpm) at a rate of 5 T / H with a volumetric continuous feeder.
동시에 표 1 및 표 2에 언급된 각각의 수성 30wt% PTFE 유제 A, B, C, D 또는 H를 16.7ks/H (PTFE 고체 5kg/H)의 속도로 계량 펌프로 공급하여 분산시키고 혼합했다.At the same time each of the aqueous 30 wt% PTFE emulsions A, B, C, D or H mentioned in Tables 1 and 2 were fed into the metering pump at a rate of 16.7ks / H (5 kg / H of PTFE solids) to disperse and mix.
PTFE를 즉시 피브릴화하고 포틀랜드 시멘트내로 균질적으로 분포시켜 연속적으로 분말 조성물을 제조했다. 작동도중 각각의 유제 A, B, C 또는 D는 200시간 동안 연속적으로 공급될 수 있으나, 비이온 계면활성제를 함유하는 유제 H는 응집된 PTFE로 펌프의 막힘을 유발하여 응집물을 제거하기 위해 15-20 시간 후에 작동의 중단을 필요로 했다.The PTFE was immediately fibrillated and distributed homogeneously into Portland cement to continuously produce a powder composition. During operation each emulsion A, B, C or D can be fed continuously for 200 hours, but emulsion H containing a non-ionic surfactant is agglomerated PTFE to cause clogging of the pump to remove aggregates. After 20 hours a break in operation was required.
시험 3Test 3
시험 1에 사용된 유제 A, B, C, D 또는 H에 의해 방진된 각각의 100g의 생석회에 1000㎖의 물을 첨가하고, 교반기로 교반하여 (초기에 열이 발생) 석회의 밀크를 제조했다. 석회의 밀크를 2일 동안 침강시키고, 유화안정제를 검출하기 위해 상청액을 액체 크로마토그래피로 분석했다. 그결과, 오직 유제 H에 대해서만 0.2% 함량의 유화안정제가 검출되었다.1000 ml of water were added to each 100 g of quicklime dusted by emulsions A, B, C, D or H used in Test 1, and stirred with a stirrer (heating initially) to prepare milk of lime. . The milk of lime was allowed to settle for 2 days and the supernatant was analyzed by liquid chromatography to detect emulsion stabilizers. As a result, an emulsion stabilizer of 0.2% content was detected only for emulsion H.
본 발명은 고 방진성(dust-preventive) 폴리테트라플루오로에틸렌 (이하 PTFE라고함) 을 사용하여 분말상물질의 분진을 억제하기 위한 방법에 관한 것이다.The present invention relates to a method for suppressing dust of a powdery substance using high dust-preventive polytetrafluoroethylene (hereinafter referred to as PTFE).
본 발명에 따른 분진억제방법은 분말상물질에 대한 향상된 방진효율을 나타내고, 지하수의 오염가능성을 감소시킨다.The dust suppression method according to the present invention shows an improved dustproofing efficiency for powdery materials and reduces the possibility of contamination of groundwater.
Claims (4)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP94-180487 | 1994-07-11 | ||
JP6180487A JP2827152B2 (en) | 1994-07-11 | 1994-07-11 | Dust suppression method |
Publications (2)
Publication Number | Publication Date |
---|---|
KR960704993A KR960704993A (en) | 1996-10-09 |
KR100351571B1 true KR100351571B1 (en) | 2003-01-24 |
Family
ID=16084095
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019960701232A KR100351571B1 (en) | 1994-07-11 | 1995-07-03 | Method of controlling dust |
Country Status (9)
Country | Link |
---|---|
US (1) | US5788879A (en) |
EP (1) | EP0770659B1 (en) |
JP (1) | JP2827152B2 (en) |
KR (1) | KR100351571B1 (en) |
AU (1) | AU692569B2 (en) |
BR (1) | BR9506031A (en) |
DE (1) | DE69526085T2 (en) |
NZ (1) | NZ288742A (en) |
WO (1) | WO1996001881A1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100982711B1 (en) * | 2005-06-29 | 2010-09-17 | 가부시키가이샤 니포 코포레이션 | Method of dust suppression disposal |
KR100982710B1 (en) | 2005-06-29 | 2010-09-17 | 듀폰-미쯔이 플루오로케미칼 가부시끼가이샤 | Dust disposal agent composition |
Families Citing this family (49)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU5136198A (en) * | 1997-12-03 | 1999-06-16 | Dupont-Mitsui Fluorochemicals Co., Ltd. | Dust prevention process for dust-generating powders |
US6358309B1 (en) * | 1998-12-10 | 2002-03-19 | 3M Innovative Properties Company | Low dust wall repair compound |
JP4117956B2 (en) * | 1998-12-24 | 2008-07-16 | 麻生ラファージュセメント株式会社 | Dust-proof cement composition with improved strength |
US6213415B1 (en) * | 1999-09-13 | 2001-04-10 | W.R. Grace & Co.-Conn. | Process for improving grinding of cement clinker in mills employing rollers |
JP4412832B2 (en) * | 2000-08-23 | 2010-02-10 | 麻生ラファージュセメント株式会社 | Dust-proof treatment method for dust-generating powder |
ITMI20021383A1 (en) * | 2002-06-21 | 2003-12-22 | Dry Doughy S R L | PROCEDURE AND ADDITIVE FOR THE COALITION AND DRY MIXING OF POWDERS UP TO ARRIVING THE SHEETING |
CA2521007C (en) * | 2003-04-15 | 2009-08-11 | Hexion Specialty Chemicals, Inc. | Particulate material containing thermoplastic elastomer and methods for making and using same |
US20060078685A1 (en) * | 2004-10-08 | 2006-04-13 | Frankpitt Graeme S | Dust suppression method and apparatus |
AU2005294760B2 (en) * | 2004-10-08 | 2011-04-07 | E.I. Du Pont De Nemours And Company | Dust suppression method and apparatus |
JP5543702B2 (en) * | 2008-07-16 | 2014-07-09 | 孝信 安間 | Dust proofing method for the ground |
JP5421331B2 (en) * | 2011-08-16 | 2014-02-19 | 株式会社Nippo | Dust suppression processing method |
JP5415496B2 (en) * | 2011-08-16 | 2014-02-12 | 株式会社Nippo | Dust suppression processing method |
JP2012077312A (en) * | 2012-01-11 | 2012-04-19 | Du Pont Mitsui Fluorochem Co Ltd | Dust treatment agent composition |
CN104220517B (en) | 2012-03-27 | 2016-08-24 | 大金工业株式会社 | Aqueous fluorine-containing polymer dispersion |
JP5937870B2 (en) | 2012-03-30 | 2016-06-22 | ダイキン工業株式会社 | Nonionic surfactant composition and aqueous fluoropolymer dispersion |
JP5954432B2 (en) | 2012-11-30 | 2016-07-20 | ダイキン工業株式会社 | Process for producing polytetrafluoroethylene aqueous dispersion |
CA3047473A1 (en) | 2016-12-23 | 2018-06-28 | Trican Well Service Ltd. | Oil-based dust suppression composition and method of use |
CN110446723B (en) | 2017-03-31 | 2021-10-12 | 大金工业株式会社 | Method for producing fluoropolymer, surfactant for polymerization, and use of surfactant |
EP3858871A1 (en) | 2017-03-31 | 2021-08-04 | Daikin Industries, Ltd. | Composition comprising a fluoropolymer |
CN107473851A (en) * | 2017-09-19 | 2017-12-15 | 四川大学 | Urban soil Dust Improvement construction technology |
CN107417474A (en) * | 2017-09-19 | 2017-12-01 | 四川大学 | Urban soil dust controlling method |
CN111699203B (en) | 2018-02-08 | 2022-07-05 | 大金工业株式会社 | Method for producing fluoropolymer, surfactant for polymerization, use of surfactant, and composition |
WO2019168183A1 (en) | 2018-03-01 | 2019-09-06 | ダイキン工業株式会社 | Method for manufacturing fluoropolymer |
CN111801359A (en) | 2018-03-07 | 2020-10-20 | 大金工业株式会社 | Method for producing fluorine-containing polymer |
JP7174272B2 (en) | 2018-11-19 | 2022-11-17 | ダイキン工業株式会社 | Method for producing modified polytetrafluoroethylene and composition |
JP7317307B2 (en) * | 2018-12-28 | 2023-07-31 | 株式会社Nippo | Dust suppression treatment method |
JP7060826B2 (en) | 2019-02-01 | 2022-04-27 | ダイキン工業株式会社 | Method for producing polytetrafluoroethylene |
JP7104354B2 (en) | 2019-02-07 | 2022-07-21 | ダイキン工業株式会社 | Composition, stretched product and method for producing the same |
CN113661184A (en) | 2019-04-16 | 2021-11-16 | 大金工业株式会社 | Method for producing fluoropolymer powder |
EP3960777A4 (en) | 2019-04-26 | 2023-01-18 | Daikin Industries, Ltd. | Fluoropolymer aqueous dispersion production method and fluoropolymer aqueous dispersion |
CN113710709A (en) | 2019-04-26 | 2021-11-26 | 大金工业株式会社 | Method for producing aqueous fluoropolymer dispersion |
WO2020218620A1 (en) | 2019-04-26 | 2020-10-29 | ダイキン工業株式会社 | Method for producing aqueous fluoropolymer dispersion, drainage treatment method, and aqueous fluoropolymer dispersion |
JP7406129B2 (en) | 2019-05-08 | 2023-12-27 | ダイキン工業株式会社 | Fluoropolymer manufacturing method and fluoropolymer |
CN118146601A (en) | 2019-07-23 | 2024-06-07 | 大金工业株式会社 | Method for producing fluorine-containing polymer, polytetrafluoroethylene composition, and polytetrafluoroethylene powder |
WO2021045228A1 (en) | 2019-09-05 | 2021-03-11 | ダイキン工業株式会社 | Polytetrafluoroethylene aqueous dispersion |
JP7231868B2 (en) | 2019-09-05 | 2023-03-02 | ダイキン工業株式会社 | Composition and method for producing same |
CN114514253A (en) | 2019-10-03 | 2022-05-17 | 大金工业株式会社 | Polytetrafluoroethylene and process for producing the same |
JP7360058B2 (en) | 2019-11-19 | 2023-10-12 | ダイキン工業株式会社 | Method of manufacturing fluoropolymer |
EP4063404A4 (en) | 2019-11-19 | 2023-12-06 | Daikin Industries, Ltd. | Method for producing fluoropolymer, method for producing polytetrafluoroethylene, method for producing perfluoroelastomer, and composition |
CN114729071A (en) | 2019-11-19 | 2022-07-08 | 大金工业株式会社 | Process for producing polytetrafluoroethylene |
JP6989792B2 (en) | 2019-12-25 | 2022-01-12 | ダイキン工業株式会社 | Fluoropolymer manufacturing method |
EP4212556A1 (en) | 2020-09-07 | 2023-07-19 | Daikin Industries, Ltd. | Aqueous modified polytetrafluoroethylene dispersion |
JPWO2022107894A1 (en) | 2020-11-19 | 2022-05-27 | ||
JPWO2022163814A1 (en) | 2021-01-28 | 2022-08-04 | ||
JPWO2022163815A1 (en) | 2021-01-28 | 2022-08-04 | ||
EP4310114A1 (en) | 2021-03-18 | 2024-01-24 | Daikin Industries, Ltd. | Method for producing fluororesin, fluororesin, and aqueous dispersion liquid |
WO2022244784A1 (en) | 2021-05-19 | 2022-11-24 | ダイキン工業株式会社 | Method for producing fluoropolymer, method for producing polytetrafluoroethylene, and composition |
EP4365211A1 (en) | 2021-06-30 | 2024-05-08 | Daikin Industries, Ltd. | Method for producing high-purity fluoropolymer-containing composition, and high-purity fluoropolymer-containing composition |
WO2023277139A1 (en) | 2021-06-30 | 2023-01-05 | ダイキン工業株式会社 | Method for producing fluoropolymer composition, and fluoropolymer composition |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3838092A (en) * | 1971-04-21 | 1974-09-24 | Kewanee Oil Co | Dustless compositions containing fiberous polytetrafluoroethylene |
US3974089A (en) * | 1971-04-21 | 1976-08-10 | The Harshaw Chemical Company | Process for preventing segregation of a component in a mixture of powders |
GB1582442A (en) * | 1976-01-22 | 1981-01-07 | Exxon Research Engineering Co | Dust laying |
JPS5712002A (en) * | 1980-06-27 | 1982-01-21 | Lion Corp | Emulsifying agent for emulsion polymerization |
US4551261A (en) * | 1984-05-07 | 1985-11-05 | Dearborn Chemical Co. | Dust suppression with elastomer-containing foam |
US4746543A (en) * | 1985-12-10 | 1988-05-24 | Zinkan Enterprises, Inc. | Composition and method for dust control |
JPS6355176A (en) * | 1986-08-27 | 1988-03-09 | 大日本インキ化学工業株式会社 | Dust-proofing coating composition for cementitious floor surface |
EP0423836B1 (en) * | 1987-09-24 | 1992-12-02 | Murakashi Lime Industry Co., Ltd | A method for dust-control treatment |
JP2538782B2 (en) * | 1987-09-24 | 1996-10-02 | 村樫石灰工業 株式会社 | Dustproof treatment method |
JP2538783B2 (en) * | 1987-09-24 | 1996-10-02 | 村樫石灰工業 株式会社 | Dustproofing composition |
JP2593697B2 (en) * | 1988-09-27 | 1997-03-26 | 三井サイテック株式会社 | Coal handling management method |
US5256444A (en) * | 1990-08-29 | 1993-10-26 | Betz Laboratories, Inc. | Method for suppressing dust emissions from bulk solids |
JP3230008B2 (en) * | 1991-12-18 | 2001-11-19 | 村樫石灰工業株式会社 | Cosmetic composition |
-
1994
- 1994-07-11 JP JP6180487A patent/JP2827152B2/en not_active Expired - Lifetime
-
1995
- 1995-07-03 BR BR9506031-6A patent/BR9506031A/en not_active IP Right Cessation
- 1995-07-03 NZ NZ288742A patent/NZ288742A/en not_active IP Right Cessation
- 1995-07-03 AU AU28081/95A patent/AU692569B2/en not_active Ceased
- 1995-07-03 KR KR1019960701232A patent/KR100351571B1/en not_active IP Right Cessation
- 1995-07-03 DE DE69526085T patent/DE69526085T2/en not_active Expired - Lifetime
- 1995-07-03 US US08/596,241 patent/US5788879A/en not_active Expired - Lifetime
- 1995-07-03 WO PCT/JP1995/001324 patent/WO1996001881A1/en active IP Right Grant
- 1995-07-03 EP EP95923571A patent/EP0770659B1/en not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100982711B1 (en) * | 2005-06-29 | 2010-09-17 | 가부시키가이샤 니포 코포레이션 | Method of dust suppression disposal |
KR100982710B1 (en) | 2005-06-29 | 2010-09-17 | 듀폰-미쯔이 플루오로케미칼 가부시끼가이샤 | Dust disposal agent composition |
Also Published As
Publication number | Publication date |
---|---|
JPH0820767A (en) | 1996-01-23 |
JP2827152B2 (en) | 1998-11-18 |
US5788879A (en) | 1998-08-04 |
NZ288742A (en) | 1997-11-24 |
AU2808195A (en) | 1996-02-09 |
EP0770659A1 (en) | 1997-05-02 |
BR9506031A (en) | 1997-10-14 |
KR960704993A (en) | 1996-10-09 |
AU692569B2 (en) | 1998-06-11 |
WO1996001881A1 (en) | 1996-01-25 |
EP0770659A4 (en) | 1997-10-08 |
EP0770659B1 (en) | 2002-03-27 |
DE69526085D1 (en) | 2002-05-02 |
DE69526085T2 (en) | 2002-11-21 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR100351571B1 (en) | Method of controlling dust | |
EP2597125B1 (en) | Method for dust-preventive treatment of material having dusting property | |
EP1918346B1 (en) | Dust disposal agent composition | |
US4128528A (en) | Clay-polymer concentrates for beneficiating clays | |
EP0848647B1 (en) | High solids lime as a caustic replacement | |
CS261247B2 (en) | Method of solid lubricants suspending | |
US4957511A (en) | Coal-water dispersion agent | |
US4601729A (en) | Aqueous phase continuous, coal fuel slurry and a method of its production | |
AU6349099A (en) | Water re-dispersible granules comprising an active matter in liquid form | |
MXPA02005725A (en) | Water-soluble air-controlling agents for cementitious compositions. | |
EP0137728B1 (en) | Water-in-oil emulsions having improved low temperature properties | |
US4417902A (en) | Process for making and composition of low viscosity coal-water slurries | |
US4605568A (en) | Application of foam to improve flow characteristics of water-insoluble products | |
US4080351A (en) | Composition and method for dispersing high molecular weight polymers in water | |
JPH11159281A (en) | Processing method of waste in slurry shielding method | |
JP7386610B2 (en) | PTFE aqueous dispersion and dust suppression treatment agent composition comprising the aqueous dispersion | |
EP0697912A1 (en) | An emulsion of oil in water | |
SU1545947A3 (en) | Coal-water suspension | |
US4492589A (en) | Anionic dispersants for aqueous slurries of carbonaceous materials | |
EP0718363B1 (en) | Aqueous fluoropolymer emulsion | |
US5608228A (en) | Rubber chemical preparation | |
RU2371463C1 (en) | Dust binding method of processing dust-forming materials | |
JPS5837089A (en) | Additive for petroleum coke/water slurry | |
WO1994020680A1 (en) | Aqueous defoamer dispersions of ethylenebis (stearamide) | |
EP0186665B1 (en) | Procedure for dispersing talc |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A201 | Request for examination | ||
E701 | Decision to grant or registration of patent right | ||
GRNT | Written decision to grant | ||
FPAY | Annual fee payment |
Payment date: 20120801 Year of fee payment: 11 |
|
FPAY | Annual fee payment |
Payment date: 20130812 Year of fee payment: 12 |
|
LAPS | Lapse due to unpaid annual fee |